PASS LP A06020250

GUDID 03613720284017

MIS STRAIGHT ROD HOLDER

MEDICREA INTERNATIONAL

Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable
Primary Device ID03613720284017
NIH Device Record Key695bf1df-f164-40bb-84dd-177e2d495c9f
Commercial Distribution StatusIn Commercial Distribution
Brand NamePASS LP
Version Model NumberA06020250
Catalog NumberA06020250
Company DUNS383228632
Company NameMEDICREA INTERNATIONAL
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS103613720284017 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


[03613720284017]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-01-20
Device Publish Date2020-01-10

On-Brand Devices [PASS LP]

03613720276043TRAUMA Ø6 mm PRE-BENT RODS - 50 TK
03613720276036TRAUMA Ø6 mm PRE-BENT RODS - 26 TK
03613720245742PEDICLE SCREWDRIVER FOR RETRIEVAL
03613720245735CANNULATED SCREWDRIVER SHAFT
03613720240846SPEEDRIVER WITH T-HANDLE
03613720224839FLEXIBLE NUTDRIVER FOR CLAW
03613720224761HOOK HOLDER
03613720224754HOOK INSERTER SET
03613720224068ROD HOLDER
03613720224006NUTDRIVER AND POSITIONNER FOR PLATE AND ROD
03613720223993SCREWDRIVER T20
03613720223986SELFHOLDING NUTDRIVER & BREAKER
03613720223979HEX HOLLOW SCREW AND NUT DRIVER 10mm
03613720223894HEXAGONAL SCREWDRIVER FOR SIMPLE SCREWS 3.5mm
03613720223887HEX HOLLOW SCREWDRIVER FOR MONOAXIAL SCREWS 6mm
03613720212287SACRAL PLATE HOLDER
03613720212270BAND HOOK HOLDER
03613720212263LIGAMENT HOOK HOLDER
03613720212249SCREWDRIVER FOR HOOK HEAD
03613720212225COUNTER HOOK HOLDER
03613720212218HOOK POST HOLDER
03613720212126NUTDRIVER SHAFT FOR DISMANTLING
03613720212119HEXAGONAL NUTDRIVER SHAFT
03613720212089ILIAC LINK HOLDER
03613720212034SPEED DRIVER
03613720212003T30 SCREWDRIVER SHAFT
03613720211983NUT HOLDER AND THREADED EXTENSION BREAKER
03613720211846PEDICLE SCREWDRIVER SHAFT FOR SHORT POST SCREW
03613720211839BASIC PEDICLE SCREWDRIVER
03613720211822PEDICLE SCREWDRIVER SHAFT FOR 1/4 POWERED DRILL DEVICE
03613720211471OPEN CONNECTOR HOLDER
03613720211440PARS HOOK HOLDER
03613720211426SACRAL SCREW HOLDER FOR T20 SCREWDRIVER
03613720211402SACRAL PLATE HOLDER
03613720211365NUTDRIVER SHAFT
03613720211358NUTDRIVER SHAFT FOR FINAL TIGHTENING
03613720211341NUTDRIVER SHAFT
03613720211334NUTDRIVER
03613720211327NUTDRIVER FOR POSITIONING HANDLE
03613720211303NUT HOLDER
03613720211105ROD HOLDER
03613720211037PASS 2 SCREWDRIVER FOR REVISION
03613720211020PEDICLE SCREWDRIVER SHAFT
03613720210788HEX HOLLOW NUTDRIVER 8mm
03613720210771HEX HOLLOW SCREWDRIVER FOR CROSSLINK SYSTEM 8mm
03613720210757T20 SCREWDRIVER SHAFT
03613720210740NUT DRIVER SHAFT FOR FINAL TIGHTENING
036137202107263.5mm HEXAGONAL SCREWDRIVER SHAFT
03613720210634PASSMED PEDICLE SCREWDRIVER FOR REVISION
03613720210627PEDICLE SCREWDRIVER SHAFT

Trademark Results [PASS LP]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PASS LP
PASS LP
79060844 3718769 Live/Registered
MEDICREA INTERNATIONAL
2008-10-10

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